The Antidepressant Vortioxetine Potently Inhibits Cell Growth in Cultured Human Glioblastoma Cells Expressing 5-HT1B
Veronica Russo1, Miriam Russo1, Maria Antonietta Oliva1
1IRCCS Neuromed, Via Atinense, 86077 Pozzilli, Italy.
Abstract:
Background: Recent evidence suggests that the antidepressant vortioxetine (Vx) inhibits the growth of glioblastoma (GBM), the most aggressive primary malignant tumor of the CNS. We used five patient-derived GBM cell lines to confirm the anti-GBM effect of Vx and explore its mechanism(s) of action. Methods: We performed in silico analysis, PCR, TUNEL assay, colony assay, and proliferation assay. Results: Vx potently inhibited GBM cell growth, and showed efficacy at concentrations of 0.1 μM that roughly correspond to therapeutic concentrations of Vx in major depression. Other antidepressants, i.e., fluoxetine and duloxetine, inhibited GBM cell growth only at high concentrations. Computational analysis showed that at least three receptor targets of Vx (5-HT7, 5-HT1D, and 5-HT1B) were expressed at moderate/high levels in GBM. The 5-HT1B receptor transcript was found in all GBM cell lines and was the only detectable Vx target in three of the five cell lines. Blocking 5-HT1B with SB224289 abolished the anti-GBM effect of Vx, even in cells expressing other Vx. Conclusions: These findings demonstrate that therapeutic concentrations of Vx inhibit GBM cell proliferation and suggest that this action may be mediated, at least in part, by 5-HT1B receptor activation.
Insights
Vortioxetine (Vx), an antidepressant, effectively inhibits glioblastoma (GBM) cell growth at therapeutic concentrations. This anti-cancer effect is primarily mediated through the 5-HT1B receptor, offering a potential new avenue for GBM treatment.
Area of Science:
- Neuro-oncology
- Pharmacology
- Molecular Biology
Background:
- Glioblastoma (GBM) is an aggressive brain tumor.
- Vortioxetine (Vx) is an antidepressant with potential anti-GBM properties.
Purpose of the Study:
- To confirm vortioxetine's anti-GBM effects.
- To investigate the mechanisms underlying vortioxetine's action against GBM cells.
Main Methods:
- In silico analysis
- Polymerase Chain Reaction (PCR)
- TUNEL assay
- Colony formation assay
- Proliferation assay
Main Results:
- Vortioxetine potently inhibited GBM cell growth at therapeutic concentrations (0.1 μM).
- The 5-HT1B receptor was expressed in all tested GBM cell lines and crucial for vortioxetine's effect.
- Blocking the 5-HT1B receptor abolished vortioxetine's anti-GBM activity.
Conclusions:
- Therapeutic concentrations of vortioxetine inhibit GBM cell proliferation.
- The 5-HT1B receptor mediates vortioxetine's anti-GBM effects.
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